01 2F. I. S. Fabrica Italiana Sintetici S. p. A.
01 1Pentazocine
02 1Pentazocine hydrochloride
01 2Italy
Registration Number : 221MF10106
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2009-06-02
Latest Date of Registration : 2017-05-19
Registration Number : 217MF10848
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2017-05-01
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PharmaCompass offers a list of Pentazocine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Pentazocine manufacturer or Pentazocine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pentazocine manufacturer or Pentazocine supplier.
PharmaCompass also assists you with knowing the Pentazocine API Price utilized in the formulation of products. Pentazocine API Price is not always fixed or binding as the Pentazocine Price is obtained through a variety of data sources. The Pentazocine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fortral manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fortral, including repackagers and relabelers. The FDA regulates Fortral manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fortral API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Fortral manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fortral supplier is an individual or a company that provides Fortral active pharmaceutical ingredient (API) or Fortral finished formulations upon request. The Fortral suppliers may include Fortral API manufacturers, exporters, distributors and traders.
click here to find a list of Fortral suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Fortral Drug Master File in Japan (Fortral JDMF) empowers Fortral API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Fortral JDMF during the approval evaluation for pharmaceutical products. At the time of Fortral JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Fortral suppliers with JDMF on PharmaCompass.
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